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United States · US · US:24338-340_3529fe2f-3c23-4862-bb20-b48026957082

Gleostine

Orange BookUNIISPLATC L01AD02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAzurity Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL01AD02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    2433834005
    1 BOTTLE in 1 CARTON (24338-340-05) / 5 CAPSULE, GELATIN COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
7BRF0Z81KG
LOMUSTINE
RxCUI 6466
Orange Book
N017588
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7BRF0Z81KG",
    "rxcui": "6466",
    "inchikey": "GQYIWUVLTXOXAJ-UHFFFAOYSA-N",
    "display_name": "LOMUSTINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3529fe2f-3c23-4862-bb20-b48026957082": {
      "match": "brand_token",
      "title": "GLEOSTINE (LOMUSTINE) CAPSULE, GELATIN COATED [AZURITY PHARMACEUTICALS, INC.]",
      "spl_version": "1",
      "published_date": "2025-11-17"
    }
  },
  "productid": "24338-340_3529fe2f-3c23-4862-bb20-b48026957082",
  "productndc": "24338-340",
  "dosage_form": "CAPSULE, GELATIN COATED",
  "orange_book": {
    "appl_no": "017588",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "5MG",
        "product_no": "004",
        "approval_date": "Dec 19, 2014"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LOMUSTINE",
  "proprietary_name": "Gleostine",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA017588",
  "marketing_category": "NDA",
  "nonproprietary_name": "lomustine",
  "start_marketing_date": "20251024",
  "active_numerator_strength": "10"
}

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